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Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices

A series of copolymers based on ε-caprolactone (ε-CL) in combination with lactone monomers substituted with alkyl groups (4 and 6 carbon atoms), specifically δ-decalactone (δ-DL), ε-decalactone (ε-DL) and δ-dodecalactone (δ-DD), as well as a copolymer using two substituted lactone monomers with alky...

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Autores principales: Ramos-Durán, Gabriela, González-Zarate, Aracely del Carmen, Enríquez-Medrano, Francisco Javier, Salinas-Hernández, Myrna, De Jesús-Téllez, Marco A., Díaz de León, Ramon, López-González, Hector Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210866/
https://www.ncbi.nlm.nih.gov/pubmed/35800320
http://dx.doi.org/10.1039/d2ra01861f
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author Ramos-Durán, Gabriela
González-Zarate, Aracely del Carmen
Enríquez-Medrano, Francisco Javier
Salinas-Hernández, Myrna
De Jesús-Téllez, Marco A.
Díaz de León, Ramon
López-González, Hector Ricardo
author_facet Ramos-Durán, Gabriela
González-Zarate, Aracely del Carmen
Enríquez-Medrano, Francisco Javier
Salinas-Hernández, Myrna
De Jesús-Téllez, Marco A.
Díaz de León, Ramon
López-González, Hector Ricardo
author_sort Ramos-Durán, Gabriela
collection PubMed
description A series of copolymers based on ε-caprolactone (ε-CL) in combination with lactone monomers substituted with alkyl groups (4 and 6 carbon atoms), specifically δ-decalactone (δ-DL), ε-decalactone (ε-DL) and δ-dodecalactone (δ-DD), as well as a copolymer using two substituted lactone monomers with alkyl groups (ε-DL and δ-DD) were synthesized in different molar ratios. The objective of the synthesis of these copolymers was to evaluate the effects of branching in the polymer backbone on the crystallinity and the thermal properties of the synthesized materials. All copolymers were obtained via ring-opening polymerization with high conversion values for both comonomers using neodymium isopropoxide (Nd(i-Pr)(3)) as the initiator, and their compositions were determined by (1)H NMR and (13)C NMR. The molar masses (M(n) and M(w)) and distributions were obtained by GPC measurements. Such measurements showed that a majority of the copolymers exhibited dispersities (Ɖ) in the range of 1.2–1.6 and M(n) in the range of 15–40 kDa. First- and second-order transitions such as melting, crystallization and glass transition, as well as the crystallization degree (melting enthalpy), were determined by DSC analysis. Copolymers based on ε-CL developed interesting behaviors, wherein the copolymers with higher percentages of this monomer exhibited semicrystalline behavior, while the copolymers with a higher percentage of the comonomers ε-DL, δ-DL or δ-DD showed amorphous behavior. In contrast, the copolymers synthesized using both monomers from the alkyl group-substituted lactone developed fully amorphous features, regardless of their composition. These changes in the crystalline features of the synthesized copolymers suggest that the content of short branchings on the copolymer backbone will significantly modify their rates of hydrolytic degradation and their potential use in the development of different soft medical devices.
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spelling pubmed-92108662022-07-06 Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices Ramos-Durán, Gabriela González-Zarate, Aracely del Carmen Enríquez-Medrano, Francisco Javier Salinas-Hernández, Myrna De Jesús-Téllez, Marco A. Díaz de León, Ramon López-González, Hector Ricardo RSC Adv Chemistry A series of copolymers based on ε-caprolactone (ε-CL) in combination with lactone monomers substituted with alkyl groups (4 and 6 carbon atoms), specifically δ-decalactone (δ-DL), ε-decalactone (ε-DL) and δ-dodecalactone (δ-DD), as well as a copolymer using two substituted lactone monomers with alkyl groups (ε-DL and δ-DD) were synthesized in different molar ratios. The objective of the synthesis of these copolymers was to evaluate the effects of branching in the polymer backbone on the crystallinity and the thermal properties of the synthesized materials. All copolymers were obtained via ring-opening polymerization with high conversion values for both comonomers using neodymium isopropoxide (Nd(i-Pr)(3)) as the initiator, and their compositions were determined by (1)H NMR and (13)C NMR. The molar masses (M(n) and M(w)) and distributions were obtained by GPC measurements. Such measurements showed that a majority of the copolymers exhibited dispersities (Ɖ) in the range of 1.2–1.6 and M(n) in the range of 15–40 kDa. First- and second-order transitions such as melting, crystallization and glass transition, as well as the crystallization degree (melting enthalpy), were determined by DSC analysis. Copolymers based on ε-CL developed interesting behaviors, wherein the copolymers with higher percentages of this monomer exhibited semicrystalline behavior, while the copolymers with a higher percentage of the comonomers ε-DL, δ-DL or δ-DD showed amorphous behavior. In contrast, the copolymers synthesized using both monomers from the alkyl group-substituted lactone developed fully amorphous features, regardless of their composition. These changes in the crystalline features of the synthesized copolymers suggest that the content of short branchings on the copolymer backbone will significantly modify their rates of hydrolytic degradation and their potential use in the development of different soft medical devices. The Royal Society of Chemistry 2022-06-21 /pmc/articles/PMC9210866/ /pubmed/35800320 http://dx.doi.org/10.1039/d2ra01861f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ramos-Durán, Gabriela
González-Zarate, Aracely del Carmen
Enríquez-Medrano, Francisco Javier
Salinas-Hernández, Myrna
De Jesús-Téllez, Marco A.
Díaz de León, Ramon
López-González, Hector Ricardo
Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title_full Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title_fullStr Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title_full_unstemmed Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title_short Synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
title_sort synthesis of copolyesters based on substituted and non-substituted lactones towards the control of their crystallinity and their potential effect on hydrolytic degradation in the design of soft medical devices
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210866/
https://www.ncbi.nlm.nih.gov/pubmed/35800320
http://dx.doi.org/10.1039/d2ra01861f
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